Trends in esophageal cancer and body mass index by race and gender in the state of Michigan
© Kort et al; licensee BioMed Central Ltd. 2009
Received: 22 December 2008
Accepted: 23 June 2009
Published: 23 June 2009
Adenocarcinoma of the esophagus has been increasing in incidence in the U.S. over the past several decades, particularly among white males. The factors driving the racial disparity in adenocarcinomas rates are not well understood.
Here we examine trends in both esophageal cancer incidence and body mass index (BMI) in a geographically defined cohort by gender and race. Age-adjusted esophageal cancer incidence rates from 1985 to 2005 were calculated from data collected by the Michigan state cancer registry. Trends were analyzed along with trends in BMI data obtained from the Behavioral Risk Factor Survey administered by the Centers for Disease Control.
Overall, age adjusted incidence rates in esophageal carcinoma increased from 4.49 to 4.72 cases/100,000 persons per year in Michigan from 1985 to 2005. Among white males, the rate of adenocarcinomas increased by 0.21 cases/100,000 per year to a maximum of 6.40 cases/100,000 in 1999, after which these rates remained constant. There was a slight but non-significant increase in the rate of adenocarcinomas among African American males, for whom the average incidence rate was 8 times lower than that for white males (0.58 vs 4.72 cases/100,000 person years). While average BMI is rising in Michigan (from 26.68 in 1988 to 30.33 in 2005), average BMI was slightly higher among African Americans on average, and the rates of increase in BMI were not different between African American males and white males.
The disparity between African American males and white males is not explained by ecological-level trends in BMI. Further research to identify the factors responsible for this disparity, possibly including anatomic fat distribution, are required.
Esophageal cancer has been increasing in incidence in the U.S. over the past several decades, despite the fact that incidence rates of the squamous cell subtype has been declining rapidly. This is the result of the even more rapid rise in incidence rates of adenocarcinoma of the esophagus [1–5]. The risk factors for squamous cell carcinoma are well understood; low income, smoking, high alcohol intake, and low intake of raw fruits and vegetables can account for up to 98% of cases of squamous cell carcinoma of the esophagus [6–8]. Furthermore, differences in these risk factors account for the much higher incidence of this tumor subtype among African American males compared to white males.
Less well understood are the factors underlying the rising incidence in adenocarcinomas of the esophagus, which is now by far the most common form of the disease. One important factor associated with the rise in incidence of adenocarcinomas is increased body mass index (BMI). A relationship between increased BMI and esophageal adenocarcinoma risk has been demonstrated in both cohort [9–11] and case control [12, 13] studies. In addition, reflux is a well defined risk factor for esophageal adenocarcinoma [8, 14], and it has traditionally been assumed that the effect of elevated BMI is etiologically mediated by reflux. However, recent evidence suggests that the relationship between BMI and reflux and esophageal adenocarcinoma is synergistic – i.e., that elevated BMI has some effects on the development of disease independent of reflux . However, it remains unclear to what extent these risk factors explain the fact that the disease is most common, and is rising most rapidly, among white males compared to other groups. Furthermore, prior case control studies have typically matched on race (precluding analysis of race in multivariate risk models) and have not stratified their analyses of BMI and esophageal carcinoma risk by race.
Understanding the temporal and geographic trends in esophageal cancer, including its relationship to BMI, will promote our ability to identify the risk factors contributing to these trends. Significant geographic variation in the incidence of esophageal cancers has been noted previously [15, 16]. In this report, our goal is to add to this body of evidence by reporting trends in gender- and race-stratified esophageal cancer rates as documented in the State of Michigan's tumor registry and to examine these trends in light of ecological BMI data.
Statutory reporting of cancer cases to the state registry has been in place in the state of Michigan since 1985. For this report, we compiled public use incidence data from this database. As the data is anonymized and in the public domain, it is exempt from IRB review. The number of cases of esophageal adenocarcinomas and squamous cell carcinoma by age, gender, and race was obtained from the public use files maintained by the registry for the years 1985–2005. Esophageal adenocarcinomas was defined as ICDO codes 81403, 81443, 81903, 82103, 82113, 82553, 82603, 82613, 82623, 82633, 83103, 83233, 84103, 84803, 84813, and 84903. Squamous cell carcinoma was defined as ICDO codes 80763, 80713, 80723, 80733, 80743, 80753, and 80763.
Incidence rates per 100,000 persons per year were calculated using Michigan population estimates obtained from the U.S. Census Bureau. Rates were age adjusted by the direct method using the 2000 Michigan population as the standard.
Change over time was summarized using two metrics: average percent change and average rate of change. Average percent change was calculated as 100 * (eβ-1) where β is the slope of the best fit regression line for the (natural) log-transformed incidence rates over time. Average rate of change was simply the slope of the best fit regression line for the non-transformed incidence rates over time.
It was our subjective impression that the rate of change in adenocarcinoma incidence shifted significantly among white males in 1999. To verify this, we performed joinpoint regression to identify the significant inflection points in this data, and analysis of covariance to confirm a statistical difference in slope before vs. after 1999.
To complement our analysis of esophageal cancer incidence rates by gender and race, we also performed an ecological analysis of body mass index using data from the CDC's Behavioral Risk Factory Survey. Michigan began participating in this survey in 1988. The BMI data from this dataset – based on self reported height and weight – provides only a crude perspective on the relationship between body mass and esophageal cancer risk; nonetheless, they represent the only retrospective state-wide sample available and we report them here to glean from them what etiologic hints we can.
The cancer registry recorded a total of 9165 individuals diagnosed with esophageal carcinoma over the 20 years studied: 4551 with squamous cell carcinoma and 4614 patients with adenocarcinoma. The overall age-adjusted incidence rates of esophageal carcinomas increased slightly over this time period, from 4.49 to 4.72 cases per 100,000 persons per year. However, the trend over time was not significant.
Rate of change in annual incidence of esophageal cancer.
Squamous Cell Carcinoma
In contrast, the incidence rates of esophageal adenocarcinoma has been relatively stable for African American males and females as well as for white females (Figure 2a, c, and 2d). The increase over time in the incidence rates for white women, while modest, was statistically significant; the trend over time for African American males and females was not significant. Consistent with previous reports, there was a substantial increase in age adjusted incidence rates of esophageal adenocarcinomas for white males (Fig 2b), among whom the rate of adenocarcinomas increased by 0.25 cases/100,000 per year to a maximum of 6.40 cases/100,000 in 1999. Consistent with inspection of the curve, joinpoint regression indicated that the most significant inflection point in the incidence rates among white males occurred in 1999 (p < 0.0001). Analysis of covariance indicated a highly significant difference in the slope of the trend line from 1985 to 1999 as compared to the trend line from 1999 to 2005 (p < 0.001). After 1999, the trend does not deviate significantly from 0 (p = 0.51).
Adenocarcinoma of the esophagus was a relatively uncommon malignancy at the start of the 21st century and is now the most common type of esophageal cancer. Over the same period of time, there has been a decrease in the incidence of squamous cell cancers of the esophagus [1–5, 18]. The etiology of this increase is unclear, but is at least is in part related to obesity and gastroesophageal reflux disease [9, 19]. The preponderance of patients affected are white males [15–17, 20]. Our results are similar to other reported studies in that we have found an epidemic increase in adenocarcinoma of the esophagus in white males.
Over the studied period the age-adjusted incidence rate of esophageal adenocarcinomas increased almost threefold while the incidence rate of squamous cell carcinomas decreased just over two fold. The increase in adenocarcinomas was most pronounced among white males, while the decrease in squamous cell carcinoma was most pronounced among African American males. These trends are similar to previous studies[1–5, 18]. However, the trend in incidence of adenocarcinomas among white males shifted in 1999. Between 1999 and 2005, there has been no significant change in incidence of adenocarcinomas among white males in Michigan.
The etiology of the increase in adenocarcinoma of the esophagus is unclear; however, it appears to be at least partly related to obesity. Multiple studies have documented an association with BMI and esophageal adenocarcinoma including several prospective case controlled studies [8–11, 17]. This has been confirmed with a metaanalysis of 2 cohort and 12 case controlled studies involving 2488 patients with adenocarcinoma esophageal cancer . The relationship between obesity and adenocarcinoma of the esophagus may be related to risk of gastroesophageal reflux disease and Barrett's esophagus. Obese patients are 2.5 times more likely to have gastroesophageal reflux disease or esophageal erosions . However, it has been suggested that elevated BMI may be etiologically related to esophageal carcinoma through mechanisms independent of GERD . Other studies indicate that central  or, more specifically, visceral  adiposity may be more relevant than overall BMI with respect to the pathogenesis of Barrett's esophagus and subsequent cancer. Finally, it has been pointed out that GERD and Barrett's esophagus may not be the only risk factors for adenocarcinoma of the esophagus in light of the very low rate of progression from GERD to Barrett's and Barrett's to carcinoma .
Jeon et al. have previously used BMI data derived from the BRFS and noted, as we did, a rise in BMI among white Americans paralleling the rise in incidence (derived from SEER data) of esophageal adenocarcinoma . This study did not report data on African Americans. We are aware of no previous report describing historical trends in BMI and esophageal cancer comparing the experience of African Americans and caucasians. While BMI has been clearly shown to be a risk factor for esophageal adenocarcinomas, it is noteworthy that African American males and white males in Michigan had similar BMIs as reported in the BRFS, and nearly identical increases in BMI over time. This analysis has several shortcomings, including the self-reported nature of the data, the sparseness of data for African Americans as indicated by the noise in the data, and ecological nature of the analysis. Nevertheless, this data demonstrates the expected rise in BMI over time, and these trends in the data are highly significant. Yet they yield no evidence that the disparity between adenocarcinoma incidence in African American males and white males can be attributed to differences in BMI. Furthermore, other risk factors (smoking, alcohol, low fruit and vegetable intake) remain somewhat more prevalent among African American males as indicated by their higher rates of squamous cell carcinoma (though these factors are rapidly improving). Finally, there was no evidence in the BRFS data that the shift in incidence trend that occurred among white males beginning in 1999 was preceded by a shift in BMI in this population.
It has been shown in previous studies that BMI-related cancer risk depends in part on the distribution of fat. There are clear gender and racial differences in the anatomic distribution of visceral fat. Whites have a high proportion of abdominal visceral fat in compared to African Americans [23, 24]. Men have been found to have greater visceral adipose tissue than women [23–25]. White men, but not white women have more visceral adipose tissue than African American men and women, and their maximum visceral adipose tissue occurred within the abdomen [25, 26]. There are several roles that visceral adipose tissue, particularly abdominal visceral adipose tissue, may play in etiology of adenocarcinoma of the esophagus. In obese patients, this pattern of obesity is related to Barrett's esophagus . Explanations for this relationship include mechanical pressure resulting in reflux. This may also be partly related to the fact that visceral adipose tissue is hormonally active and associated with metabolic derangements .
The incidence rate of esophageal adenocarcinoma has increased in Michigan between 1985 and 2005. This increase ceased in 1999 for white males. African Americans continue to demonstrate a rapid decline in the incidence of squamous cell carcinoma, as do the other groups examined – albeit to a lesser extent. Although mean BMI increased throughout the study, the pattern of change does not explain why adenocarcinoma is more common and was increasing more rapidly during most of the observed period among white males as compared to African American males. These findings suggest that factors in addition to BMI are responsible for the differences in incidence rates between African American males and white males. These factors may include fat distribution and/or other risk factors yet to be identified.
Behavioral Risk Factor Survey
Body Mass Index
Gastroesophageal Reflux Disease
Surveillance, Epidemiology, and End Results program
This work was supported by the Jay and Betty Van Andel Foundation, and by the National Institute of Child Health and Human Development (T32 program grant #HD046377-01A1)
- Wei JT, Shaheen N: The changing epidemiology of esophageal adenocarcinoma. Semin Gastrointest Dis. 2003, 14 (3): 112-127.PubMedGoogle Scholar
- Pera M, Cameron AJ, Trastek VF, Carpenter HA, Zinsmeister AR: Increasing incidence of adenocarcinoma of the esophagus and esophagogastric junction. Gastroenterology. 1993, 104 (2): 510-513.PubMedGoogle Scholar
- Devesa SS, Blot WJ, Fraumeni JF: Changing patterns in the incidence of esophageal and gastric carcinoma in the United States. Cancer. 1998, 83 (10): 2049-2053. 10.1002/(SICI)1097-0142(19981115)83:10<2049::AID-CNCR1>3.0.CO;2-2.View ArticlePubMedGoogle Scholar
- Chen MY, Ott DJ, Gelfand DW: More evidence for the increasing prevalence of adenocarcinoma of the esophagus over an 18-year period. J Clin Gastroenterol. 1995, 21 (3): 254-255. 10.1097/00004836-199510000-00019.View ArticlePubMedGoogle Scholar
- Blot WJ, Devesa SS, Kneller RW, Fraumeni JF: Rising incidence of adenocarcinoma of the esophagus and gastric cardia. JAMA. 1991, 265 (10): 1287-1289. 10.1001/jama.265.10.1287.View ArticlePubMedGoogle Scholar
- Brown LM, Hoover R, Silverman D, Baris D, Hayes R, Swanson GM, Schoenberg J, Greenberg R, Liff J, Schwartz A, et al: Excess incidence of squamous cell esophageal cancer among US Black men: role of social class and other risk factors. Am J Epidemiol. 2001, 153 (2): 114-122. 10.1093/aje/153.2.114.View ArticlePubMedGoogle Scholar
- Freedman ND, Park Y, Subar AF, Hollenbeck AR, Leitzmann MF, Schatzkin A, Abnet CC: Fruit and vegetable intake and esophageal cancer in a large prospective cohort study. Int J Cancer. 2007, 121 (12): 2753-2760. 10.1002/ijc.22993.View ArticlePubMedGoogle Scholar
- Engel LS, Chow WH, Vaughan TL, Gammon MD, Risch HA, Stanford JL, Schoenberg JB, Mayne ST, Dubrow R, Rotterdam H, et al: Population attributable risks of esophageal and gastric cancers. J Natl Cancer Inst. 2003, 95 (18): 1404-1413.View ArticlePubMedGoogle Scholar
- MacInnis RJ, English DR, Hopper JL, Giles GG: Body size and composition and the risk of gastric and oesophageal adenocarcinoma. Int J Cancer. 2006, 118 (10): 2628-2631. 10.1002/ijc.21638.View ArticlePubMedGoogle Scholar
- Merry AH, Schouten LJ, Goldbohm RA, Brandt van den PA: Body mass index, height and risk of adenocarcinoma of the oesophagus and gastric cardia: a prospective cohort study. Gut. 2007, 56 (11): 1503-1511. 10.1136/gut.2006.116665.View ArticlePubMedPubMed CentralGoogle Scholar
- Ryan AM, Rowley SP, Fitzgerald AP, Ravi N, Reynolds JV: Adenocarcinoma of the oesophagus and gastric cardia: male preponderance in association with obesity. Eur J Cancer. 2006, 42 (8): 1151-1158. 10.1016/j.ejca.2005.12.024.View ArticlePubMedGoogle Scholar
- Whiteman DC, Sadeghi S, Pandeya N, Smithers BM, Gotley DC, Bain CJ, Webb PM, Green AC: Combined effects of obesity, acid reflux and smoking on the risk of adenocarcinomas of the oesophagus. Gut. 2008, 57 (2): 173-180. 10.1136/gut.2007.131375.View ArticlePubMedGoogle Scholar
- Lindblad M, Rodriguez LA, Lagergren J: Body mass, tobacco and alcohol and risk of esophageal, gastric cardia, and gastric non-cardia adenocarcinoma among men and women in a nested case-control study. Cancer Causes Control. 2005, 16 (3): 285-294. 10.1007/s10552-004-3485-7.View ArticlePubMedGoogle Scholar
- Kubo A, Corley DA: Body mass index and adenocarcinomas of the esophagus or gastric cardia: a systematic review and meta-analysis. Cancer Epidemiol Biomarkers Prev. 2006, 15 (5): 872-878. 10.1158/1055-9965.EPI-05-0860.View ArticlePubMedGoogle Scholar
- Bollschweiler E, Wolfgarten E, Gutschow C, Holscher AH: Demographic variations in the rising incidence of esophageal adenocarcinoma in white males. Cancer. 2001, 92 (3): 549-555. 10.1002/1097-0142(20010801)92:3<549::AID-CNCR1354>3.0.CO;2-L.View ArticlePubMedGoogle Scholar
- Kubo A, Corley DA: Marked regional variation in adenocarcinomas of the esophagus and the gastric cardia in the United States. Cancer. 2002, 95 (10): 2096-2102. 10.1002/cncr.10940.View ArticlePubMedGoogle Scholar
- Pera M, Manterola C, Vidal O, Grande L: Epidemiology of esophageal adenocarcinoma. J Surg Oncol. 2005, 92 (3): 151-159. 10.1002/jso.20357.View ArticlePubMedGoogle Scholar
- El-Serag HB, Mason AC, Petersen N, Key CR: Epidemiological differences between adenocarcinoma of the oesophagus and adenocarcinoma of the gastric cardia in the USA. Gut. 2002, 50 (3): 368-372. 10.1136/gut.50.3.368.View ArticlePubMedPubMed CentralGoogle Scholar
- El-Serag HB, Kvapil P, Hacken-Bitar J, Kramer JR: Abdominal obesity and the risk of Barrett's esophagus. Am J Gastroenterol. 2005, 100 (10): 2151-2156. 10.1111/j.1572-0241.2005.00251.x.View ArticlePubMedGoogle Scholar
- Vega KJ, Jamal MM: Changing pattern of esophageal cancer incidence in New Mexico. Am J Gastroenterol. 2000, 95 (9): 2352-2356. 10.1111/j.1572-0241.2000.02329.x.View ArticlePubMedGoogle Scholar
- Edelstein ZR, Farrow DC, Bronner MP, Rosen SN, Vaughan TL: Central adiposity and risk of Barrett's esophagus. Gastroenterology. 2007, 133 (2): 403-411. 10.1053/j.gastro.2007.05.026.View ArticlePubMedGoogle Scholar
- Jeon J, Luebeck EG, Moolgavkar SH: Age effects and temporal trends in adenocarcinoma of the esophagus and gastric cardia (United States). Cancer Causes Control. 2006, 17 (7): 971-981. 10.1007/s10552-006-0037-3.View ArticlePubMedGoogle Scholar
- Stanforth PR, Jackson AS, Green JS, Gagnon J, Rankinen T, Despres JP, Bouchard C, Leon AS, Rao DC, Skinner JS, et al: Generalized abdominal visceral fat prediction models for black and white adults aged 17–65 y: the HERITAGE Family Study. Int J Obes Relat Metab Disord. 2004, 28 (7): 925-932. 10.1038/sj.ijo.0802563.View ArticlePubMedGoogle Scholar
- Conway JM, Yanovski SZ, Avila NA, Hubbard VS: Visceral adipose tissue differences in black and white women. Am J Clin Nutr. 1995, 61 (4): 765-771.PubMedGoogle Scholar
- Demerath EW, Sun SS, Rogers N, Lee M, Reed D, Choh AC, Couch W, Czerwinski SA, Chumlea WC, Siervogel RM, et al: Anatomical patterning of visceral adipose tissue: race, sex, and age variation. Obesity (Silver Spring). 2007, 15 (12): 2984-2993. 10.1038/oby.2007.356.View ArticleGoogle Scholar
- Hoffman DJ, Wang Z, Gallagher D, Heymsfield SB: Comparison of visceral adipose tissue mass in adult African Americans and whites. Obes Res. 2005, 13 (1): 66-74. 10.1038/oby.2005.9.View ArticlePubMedGoogle Scholar
- Bacha F, Saad R, Gungor N, Janosky J, Arslanian SA: Obesity, regional fat distribution, and syndrome X in obese black versus white adolescents: race differential in diabetogenic and atherogenic risk factors. J Clin Endocrinol Metab. 2003, 88 (6): 2534-2540. 10.1210/jc.2002-021267.View ArticlePubMedGoogle Scholar
- Kim HJ, Fay MP, Feuer EJ, Midthune DN: Permutation tests for joinpoint regression with applications to cancer rates. Stat Med. 2000, 19 (3): 335-351. 10.1002/(SICI)1097-0258(20000215)19:3<335::AID-SIM336>3.0.CO;2-Z.View ArticlePubMedGoogle Scholar
- Ihaka R, Gentleman R: R: A language for data analysis and graphics. J Comput Graph Stat. 1996, 5: 299-314. 10.2307/1390807.Google Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-230X/9/47/prepub
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